Zika virus has oncolytic activity against glioblastoma stem cells

Author:

Zhu Zhe12ORCID,Gorman Matthew J.3,McKenzie Lisa D.45,Chai Jiani N.4ORCID,Hubert Christopher G.2,Prager Briana C.2,Fernandez Estefania3,Richner Justin M.4,Zhang Rong4,Shan Chao67,Tycksen Eric8,Wang Xiuxing12ORCID,Shi Pei-Yong67,Diamond Michael S.34910ORCID,Rich Jeremy N.12,Chheda Milan G.45ORCID

Affiliation:

1. Department of Medicine, Division of Regenerative Medicine, University of California, San Diego, School of Medicine, La Jolla, CA

2. Department of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH

3. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO

4. Department of Medicine, Washington University School of Medicine, St. Louis, MO

5. Department of Neurology, Washington University School of Medicine, St. Louis, MO

6. Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX

7. Department of Pharmacology and Toxicology, Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, TX

8. Genome Technology Access Center, Department of Genetics, Washington University in St. Louis, St. Louis, MO

9. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO

10. The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO

Abstract

Glioblastoma is a highly lethal brain cancer that frequently recurs in proximity to the original resection cavity. We explored the use of oncolytic virus therapy against glioblastoma with Zika virus (ZIKV), a flavivirus that induces cell death and differentiation of neural precursor cells in the developing fetus. ZIKV preferentially infected and killed glioblastoma stem cells (GSCs) relative to differentiated tumor progeny or normal neuronal cells. The effects against GSCs were not a general property of neurotropic flaviviruses, as West Nile virus indiscriminately killed both tumor and normal neural cells. ZIKV potently depleted patient-derived GSCs grown in culture and in organoids. Moreover, mice with glioblastoma survived substantially longer and at greater rates when the tumor was inoculated with a mouse-adapted strain of ZIKV. Our results suggest that ZIKV is an oncolytic virus that can preferentially target GSCs; thus, genetically modified strains that further optimize safety could have therapeutic efficacy for adult glioblastoma patients.

Funder

National Institutes of Health

Elsa U. Pardee Foundation

Concern Foundation

Cancer Research Foundation

Washington University

NCI

National Center for Research Resources

NIH

National Center for Advancing Translational Sciences

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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